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首页> 外文期刊>Journal of the Indian Chemical Society >Carbon-carbon bond formation via palladium catalyzed reactions of organomercurials with acylhalides
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Carbon-carbon bond formation via palladium catalyzed reactions of organomercurials with acylhalides

机译:通过有机汞与酰基卤的钯催化反应形成碳-碳键

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摘要

The palladium catalyzed acyldemetallation reactions of methyl mercury iodide provide a mild,selective and general method for the construction of new C-C bond i.e.for the synthesis of unsymmetrical ketone.The reaction proceeds in acetone,in the presence of a nucleophilic catalyst (iodide ion),at room temperature.The catalytic cycle involved in the reaction consists of a sequence of oxidative addition,transmetallation and reductive elimination steps.The role played by the iodide ion as a nucleophilic catalyst is discussed.
机译:甲基碘甲烷的钯催化的酰基脱金属反应为构建新的CC键(即合成不对称酮)提供了温和,选择性和通用的方法。该反应在丙酮中,亲核催化剂(碘离子)存在下进行,反应中涉及的催化循环由一系列的氧化加成,金属间转移和还原消除步骤组成。讨论了碘离子作为亲核催化剂的作用。

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